Literature DB >> 14681753

Characterization of brain malformations in the Baraitser-Winter syndrome and review of the literature.

M Rossi1, R Guerrini, W B Dobyns, G Andria, R M Winter.   

Abstract

Baraitser-Winter syndrome is a rare autosomal recessive disorder characterized by developmental delay, dysmorphic features, and multiple malformations also involving the brain. We report a further case and provide updated information about an unrelated girl reported in the original paper by Baraitser and Winter. Both of them presented with pachygyria and the latter case was recently found to have subcortical band heterotopia on high resolution brain MRI imaging. These two patients and a review of the previously reported cases indicate that a specific pattern of brain anomalies falling in the agyria-pachygyria-band spectrum is associated with this dysmorphic syndrome, which may be considered another example of syndromic neuronal migration defect.

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Year:  2003        PMID: 14681753     DOI: 10.1055/s-2003-44666

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  7 in total

Review 1.  Comprehensive genotype-phenotype correlation in lissencephaly.

Authors:  Ai Peng Tan; Wui Khean Chong; Kshitij Mankad
Journal:  Quant Imaging Med Surg       Date:  2018-08

2.  Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia.

Authors:  Eden V Haverfield; Amanda J Whited; Kristin S Petras; William B Dobyns; Soma Das
Journal:  Eur J Hum Genet       Date:  2008-12-03       Impact factor: 4.246

3.  A novel mutation in ACTG1 causing Baraitser-Winter syndrome with extremely variable expressivity in three generations.

Authors:  Andrew Kemerley; Christina Sloan; Wanda Pfeifer; Richard Smith; Arlene Drack
Journal:  Ophthalmic Genet       Date:  2016-04-20       Impact factor: 1.803

4.  Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases.

Authors:  Alain Verloes; Nataliya Di Donato; Julien Masliah-Planchon; Marjolijn Jongmans; Omar A Abdul-Raman; Beate Albrecht; Judith Allanson; Han Brunner; Debora Bertola; Nicolas Chassaing; Albert David; Koen Devriendt; Pirayeh Eftekhari; Valérie Drouin-Garraud; Francesca Faravelli; Laurence Faivre; Fabienne Giuliano; Leina Guion Almeida; Jorge Juncos; Marlies Kempers; Hatice Koçak Eker; Didier Lacombe; Angela Lin; Grazia Mancini; Daniela Melis; Charles Marques Lourenço; Victoria Mok Siu; Gilles Morin; Marjan Nezarati; Malgorzata J M Nowaczyk; Jeanette C Ramer; Sara Osimani; Nicole Philip; Mary Ella Pierpont; Vincent Procaccio; Zeichi-Seide Roseli; Massimiliano Rossi; Cristina Rusu; Yves Sznajer; Ludivine Templin; Vera Uliana; Mirjam Klaus; Bregje Van Bon; Conny Van Ravenswaaij; Bruce Wainer; Andrew E Fry; Andreas Rump; Alexander Hoischen; Séverine Drunat; Jean-Baptiste Rivière; William B Dobyns; Daniela T Pilz
Journal:  Eur J Hum Genet       Date:  2014-07-23       Impact factor: 4.246

5.  De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome.

Authors:  Jean-Baptiste Rivière; Bregje W M van Bon; Alexander Hoischen; Stanislav S Kholmanskikh; Brian J O'Roak; Christian Gilissen; Sabine Gijsen; Christopher T Sullivan; Susan L Christian; Omar A Abdul-Rahman; Joan F Atkin; Nicolas Chassaing; Valerie Drouin-Garraud; Andrew E Fry; Jean-Pierre Fryns; Karen W Gripp; Marlies Kempers; Tjitske Kleefstra; Grazia M S Mancini; Małgorzata J M Nowaczyk; Conny M A van Ravenswaaij-Arts; Tony Roscioli; Michael Marble; Jill A Rosenfeld; Victoria M Siu; Bert B A de Vries; Jay Shendure; Alain Verloes; Joris A Veltman; Han G Brunner; M Elizabeth Ross; Daniela T Pilz; William B Dobyns
Journal:  Nat Genet       Date:  2012-02-26       Impact factor: 38.330

Review 6.  A developmental and genetic classification for malformations of cortical development: update 2012.

Authors:  A James Barkovich; Renzo Guerrini; Ruben I Kuzniecky; Graeme D Jackson; William B Dobyns
Journal:  Brain       Date:  2012-03-16       Impact factor: 13.501

7.  Baraitser and Winter syndrome with growth hormone deficiency.

Authors:  Farida Chentli; Hadjer Zellagui
Journal:  J Pediatr Neurosci       Date:  2014 Sep-Dec
  7 in total

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